Petrov V - Search Results

1

Partial deficiency of 17α-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif.

Rubtsov P, Nizhnik A, Dedov I, Kalinchenko N, Petrov V, Orekhova A, Spirin P, Prassolov V, Tiulpakov A. Rubtsov P, et al. Among authors: petrov v. Eur J Endocrinol. 2015 May;172(5):K19-25. doi: 10.1530/EJE-14-0834. Epub 2015 Feb 3. Eur J Endocrinol. 2015. PMID: 25650406

2

Minigene splicing assessment of 20 novel synonymous and intronic glucokinase gene variants identified in patients with maturity-onset diabetes of the young.

Tiulpakov A, Zubkova N, Makretskaya N, Krasnova TS, Melnikova AI, Fedyaeva AS, Vasilyev E, Petrov VM, Rubtsov PM. Tiulpakov A, et al. Hum Mutat. 2020 Jan;41(1):129-132. doi: 10.1002/humu.23919. Epub 2019 Nov 15. Hum Mutat. 2020. PMID: 31529753

3

Familial Acromegaly and Bilateral Asynchronous Pheochromocytomas in a Female Patient With a MAX Mutation: A Case Report.

Mamedova E, Vasilyev E, Petrov V, Buryakina S, Tiulpakov A, Belaya Z. Mamedova E, et al. Among authors: petrov v. Front Endocrinol (Lausanne). 2021 May 31;12:683492. doi: 10.3389/fendo.2021.683492. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34135865 Free PMC article.

4

Primary hyperparathyroidism in young patients in Russia: high frequency of hyperparathyroidism-jaw tumor syndrome.

Mamedova E, Mokrysheva N, Vasilyev E, Petrov V, Pigarova E, Kuznetsov S, Kuznetsov N, Rozhinskaya L, Melnichenko G, Dedov I, Tiulpakov A. Mamedova E, et al. Among authors: petrov v. Endocr Connect. 2017 Nov;6(8):557-565. doi: 10.1530/EC-17-0126. Epub 2017 Sep 4. Endocr Connect. 2017. PMID: 28870973 Free PMC article.

5

High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.

Makretskaya N, Bezlepkina O, Kolodkina A, Kiyaev A, Vasilyev EV, Petrov V, Kalinenkova S, Malievsky O, Dedov II, Tiulpakov A. Makretskaya N, et al. Among authors: petrov v. PLoS One. 2018 Sep 21;13(9):e0204323. doi: 10.1371/journal.pone.0204323. eCollection 2018. PLoS One. 2018. PMID: 30240412 Free PMC article.

6

Second-hit APC mutation in a familial adamantinomatous craniopharyngioma.

Gorelyshev A, Mazerkina N, Medvedeva O, Vasilyev E, Petrov V, Ryzhova M, Gorelyshev S, Tiulpakov A. Gorelyshev A, et al. Among authors: petrov v. Neuro Oncol. 2020 Jun 9;22(6):889-891. doi: 10.1093/neuonc/noaa060. Neuro Oncol. 2020. PMID: 32170310 Free PMC article. No abstract available.

7

High frequency of pathogenic and rare sequence variants in diabetes-related genes among Russian patients with diabetes in pregnancy.

Zubkova N, Burumkulova F, Plechanova M, Petrukhin V, Petrov V, Vasilyev E, Panov A, Sorkina E, Ulyatovskaya V, Makretskaya N, Tiulpakov A. Zubkova N, et al. Among authors: petrov v. Acta Diabetol. 2019 Apr;56(4):413-420. doi: 10.1007/s00592-018-01282-6. Epub 2019 Jan 20. Acta Diabetol. 2019. PMID: 30663027

8

Progressive Generalized Lipodystrophy as a Manifestation of Autoimmune Polyglandular Syndrome Type 1.

Sorkina E, Frolova E, Rusinova D, Polyakova S, Roslavtseva E, Vasilyev E, Petrov V, Tiulpakov A. Sorkina E, et al. Among authors: petrov v. J Clin Endocrinol Metab. 2016 Apr;101(4):1344-7. doi: 10.1210/jc.2015-3722. Epub 2016 Feb 18. J Clin Endocrinol Metab. 2016. PMID: 26891119

9

Gamma-ray dose threshold for MAPbI₃ solar cells.

Boldyreva AG, Novikov AV, Petrov VG, Zhivchikova AN, Tepliakova MM, Stevenson KJ. Boldyreva AG, et al. Among authors: petrov vg. Phys Chem Chem Phys. 2024 Apr 24;26(16):12372-12378. doi: 10.1039/d4cp00524d. Phys Chem Chem Phys. 2024. PMID: 38619368

10

Enhanced Solubility of Ibuprofen by Complexation with β-Cyclodextrin and Citric Acid.

Sarafska T, Ivanova S, Dudev T, Tzachev C, Petrov V, Spassov T. Sarafska T, et al. Among authors: petrov v. Molecules. 2024 Apr 6;29(7):1650. doi: 10.3390/molecules29071650. Molecules. 2024. PMID: 38611930 Free PMC article.

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